NDC 68462-127 – Gabapentin
Gabapentin 800 mg/1 · Tablet · Oral
Product NDC68462-127
Product details
- Brand name
- Gabapentin
- Generic name
- Gabapentin
- Labeler
- Glenmark Pharmaceuticals Inc., USA
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA077662
- Marketed since
- April 1, 2006
- Listing expires
- December 31, 2026
Active ingredients
- Gabapentin 800 mg/1
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 68462-127-01 | 100 TABLET in 1 BOTTLE (68462-127-01) | Apr 1, 2006 |
| 68462-127-05 | 500 TABLET in 1 BOTTLE (68462-127-05) | Apr 1, 2006 |
Recalls mentioning this NDC
- D-0320-2025 Apr 16, 2025 · Class II
CGMP Deviations - D-329-2013 May 22, 2013 · Class III
Chemical Contamination: Gabapentin Sodium tablets is recalled due to complaints related to an off - odor described as moldy, musty or fishy in nature.
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